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Dacomitinib + Pemetrexed for Patients With Advanced Non-squamous Non-small Cell Lung Cancer (NSCLC)

12 décembre 2019 mis à jour par: Central European Cooperative Oncology Group

Dacomitinib + Pemetrexed for Patients With Advanced Non-squamous Non-small Cell Lung Cancer (NSCLC): a Phase I Trial to Identify a Dose of Dacomitinib in Combination With Pemetrexed That is Safe and Tolerated as Determined by the Incidence of Dose Limiting Toxicities (DLTs)

To identify a dose of dacomitinib in combination with pemetrexed that is safe and tolerated as determined by the incidence of DLTs (dose limiting toxicities).

Aperçu de l'étude

Statut

Résilié

Intervention / Traitement

Description détaillée

This open label phase Ib trial aims to determine the safety, tolerability, the pharmacokinetic profile, and to identify a dose of dacomitinib in combination with pemetrexed.

Three sites in Austria will participate in this study. Six to nine patients will initially be enrolled to receive the target dose of 45 mg qd dacomitinib (starting from day 2 of first cycle) in combination with pemetrexed (500 mg/m² 10 min infusion, once every 3 weeks). One cycle is defined as 21 days.

The first 3 subjects will be enrolled at a rate of ≤ 1 subject per week. If the target dose regimen is safe based on the incidence of DLT another 3 subjects will be enrolled.

If the dose of 45 mg qd is not safe alternate lower doses will be explored (dose level -1, dose level -2) to identify the maximal tolerated dose (MTD) of dacomitinib in combination of pemetrexed. Six to nine patients per dose level will be enrolled.

Type d'étude

Interventionnel

Inscription (Réel)

5

Phase

  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

      • Graz, L'Autriche
        • Medizinische Universität Graz Klinische Abteilung für Onkologie
      • Innsbruck, L'Autriche
        • Universitätsklinik für Innere Medizin I

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans et plus (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

Inclusion criteria:

  • Written informed consent
  • Histologically or cytologically confirmed stage IV non-squamous NSCLC
  • Patients who are candidates to receive pemetrexed monotherapy
  • If pemetrexed has been administered as first line therapy there must be a treatment free interval of at least one cycle (21 days)
  • Measurable disease by RECIST criteria version 1.1.
  • ≥18 years of age
  • Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0-2
  • Adequate left ventricular ejection fraction (LVEF) ≥ 50% by either echocardiogram or multigated acquisition scan (MUGA)
  • Adequate organ function, including:

    1. Adequate bone marrow reserve: absolute neutrophil count (ANC) should be ≥ 1500 cells/mm3, platelets should be ≥ 100.000 cells/mm3
    2. Creatinine clearance ≥ 45 mL/min
    3. Total bilirubin ≤ 1.5 x upper normal limit (ULN)
    4. Aspartate Aminotransferase (AST) (SGOT) ≤ 3 x ULN (≤ 5.0 x ULN if hepatic metastases)
    5. Alanine Aminotransferase (ALT) (SGPT) ≤ 3 x ULN (≤ 5.0 x ULN if hepatic metastases)
  • Female patients or their partners must be postmenopausal (defined as 12 months of amenorrhea following last menses), surgically sterile or must agree to use effective contraception while receiving trial treatment and for at least 3 months thereafter (the definition of effective contraception will be based on the judgment of the investigator). Male patients or their partners must be surgically sterile or must agree to use a barrier method of contraception while receiving trial treatment and for at least 3 months thereafter. (In all cases the definition of effective contraception will be based on the judgment of the investigator).
  • Able to comply with required protocol procedures and able to receive oral medications

Exclusion criteria:

  • Any evidence of mixed histology that includes elements of small cell or carcinoid lung cancer
  • Predominantly squamous cell histology
  • Patients with symptomatic brain metastases
  • Chemotherapy, radiotherapy, biological or investigational agents within two weeks of baseline disease assessments
  • Patients with uncontrolled or significant cardiovascular disease, including:

    1. Myocardial infarction within 12 months
    2. Uncontrolled angina within 6 months
    3. Congestive heart failure within 6 months
    4. Diagnosed or suspected congenital long QT syndrome
    5. Any history of clinically significant ventricular arrhythmias (such as ventricular tachycardia, ventricular fibrillation, or Torsades de pointes)
    6. Prolonged QTc interval on pre-entry electrocardiogram. QTc must be less than CTC Grade 2 (≤480 msec) using appropriate correction formula with manual read by investigator if required. The echocardiogram (ECG) may be repeated for evaluation of eligibility after management of correctable causes for observed QTc prolongation
    7. Any history of second or third degree heart block (may be eligible if currently have a pacemaker)
    8. Heart rate <50/minute on baseline electrocardiogram
    9. Uncontrolled hypertension
  • Prior malignancy: Patients will not be eligible if they have evidence of other malignancy (other than non-melanoma skin cancer or in situ cervical cancer, or localized and presumed cured prostate cancer with prostate specific antigen (PSA) < ULN) within the last 3 years.
  • Pregnant or lactating females. Serum pregnancy test to be assessed within 7 days prior to study treatment start. Known hypersensitivity to pemetrexed and/or dacomitinib
  • Patients with exposure to other investigational drug therapy
  • Previous therapy with an oral tyrosine kinase inhibitor (TKI)

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: N / A
  • Modèle interventionnel: Affectation à un seul groupe
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Dacomitinib, Pemetrexed
Pemetrexed 500mg/m2 (i.v) q21d Dacomitinib 45mg/ orally (continuous)
Pemetrexed 500mg/m2 i.v (q21d) Dacomitinib 45mg orally (continuous)
Autres noms:
  • Alimta

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Dose Limiting Toxicities (DLTs)
Délai: From start of treatment to end of treatment or death, whichever occurs first. The study was suspended after 36 months.
The primary objective of this study is to determine the maximal tolerated dose (MTD) of the combination pemetrexed + dacomitinib by the incidence of dose limiting toxicities (DLTs).
From start of treatment to end of treatment or death, whichever occurs first. The study was suspended after 36 months.

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Overall Response Rate
Délai: Until progression of disease (PD) or 24 month after end of treatment for participants with no PD. The study was suspended after 36 months
Overall Response Rate (ORR) is defined as the proportion of patients with complete Response (CR) or partial Response (PR).
Until progression of disease (PD) or 24 month after end of treatment for participants with no PD. The study was suspended after 36 months
Overall Survival
Délai: until date of death. The study was suspended after 36 months.
Overall survival (OS) defined as time from start of Dacomitinib to date of death from any cause. Patients without recorded death were censored at the date the patient was last known to be alive. Patients were followed up for survival for 24 month after end of Treatment.
until date of death. The study was suspended after 36 months.
Progression-free Survival
Délai: Up to progression or death due to any cause. The study was suspended after 36 months
Progression-free survival (PFS) defined as time from start of Dacomitinib to date of progression or date of death from any cause, whichever occurred first. Patients without recorded progression or death were censored at the last date they were known to have not progressed. Patients were followed up for progression-free survival for 24 month after end of Treatment.
Up to progression or death due to any cause. The study was suspended after 36 months

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Chercheur principal: Christoph C Zielinski, Univ. Prof., Univ Clinic for Internal Medicine I, Dep of Oncology, Medical University of Vienna

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude

30 juillet 2013

Achèvement primaire (Réel)

15 septembre 2016

Achèvement de l'étude (Réel)

15 septembre 2016

Dates d'inscription aux études

Première soumission

27 mai 2013

Première soumission répondant aux critères de contrôle qualité

7 août 2013

Première publication (Estimation)

8 août 2013

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

30 décembre 2019

Dernière mise à jour soumise répondant aux critères de contrôle qualité

12 décembre 2019

Dernière vérification

1 janvier 2018

Plus d'information

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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